WO2016052671A1 - Film intermédiaire pour verre feuilleté et verre feuilleté - Google Patents

Film intermédiaire pour verre feuilleté et verre feuilleté Download PDF

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Publication number
WO2016052671A1
WO2016052671A1 PCT/JP2015/077863 JP2015077863W WO2016052671A1 WO 2016052671 A1 WO2016052671 A1 WO 2016052671A1 JP 2015077863 W JP2015077863 W JP 2015077863W WO 2016052671 A1 WO2016052671 A1 WO 2016052671A1
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Prior art keywords
layer
laminated glass
less
weight
polyvinyl acetal
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PCT/JP2015/077863
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English (en)
Japanese (ja)
Inventor
郁 三箇山
康晴 永井
Original Assignee
積水化学工業株式会社
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Application filed by 積水化学工業株式会社 filed Critical 積水化学工業株式会社
Priority to US15/505,240 priority Critical patent/US20170266928A1/en
Priority to JP2015549878A priority patent/JPWO2016052671A1/ja
Priority to KR1020167027696A priority patent/KR20170063431A/ko
Priority to MX2017002639A priority patent/MX2017002639A/es
Priority to EP15845570.9A priority patent/EP3202728A4/fr
Priority to CN201580036823.2A priority patent/CN106660867A/zh
Priority to BR112017003531A priority patent/BR112017003531A2/pt
Publication of WO2016052671A1 publication Critical patent/WO2016052671A1/fr

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    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00Layered products comprising a layer of synthetic resin
    • B32B27/30Layered products comprising a layer of synthetic resin comprising vinyl (co)polymers; comprising acrylic (co)polymers
    • B32B27/306Layered products comprising a layer of synthetic resin comprising vinyl (co)polymers; comprising acrylic (co)polymers comprising vinyl acetate or vinyl alcohol (co)polymers
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B17/00Layered products essentially comprising sheet glass, or glass, slag, or like fibres
    • B32B17/06Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material
    • B32B17/10Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin
    • B32B17/10005Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing
    • B32B17/10009Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing characterized by the number, the constitution or treatment of glass sheets
    • B32B17/10036Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing characterized by the number, the constitution or treatment of glass sheets comprising two outer glass sheets
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B17/00Layered products essentially comprising sheet glass, or glass, slag, or like fibres
    • B32B17/06Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material
    • B32B17/10Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin
    • B32B17/10005Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing
    • B32B17/1055Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing characterized by the resin layer, i.e. interlayer
    • B32B17/10605Type of plasticiser
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B17/00Layered products essentially comprising sheet glass, or glass, slag, or like fibres
    • B32B17/06Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material
    • B32B17/10Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin
    • B32B17/10005Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing
    • B32B17/1055Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing characterized by the resin layer, i.e. interlayer
    • B32B17/10761Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing characterized by the resin layer, i.e. interlayer containing vinyl acetal
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B17/00Layered products essentially comprising sheet glass, or glass, slag, or like fibres
    • B32B17/06Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material
    • B32B17/10Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin
    • B32B17/10005Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing
    • B32B17/1055Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing characterized by the resin layer, i.e. interlayer
    • B32B17/1077Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing characterized by the resin layer, i.e. interlayer containing polyurethane
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B17/00Layered products essentially comprising sheet glass, or glass, slag, or like fibres
    • B32B17/06Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material
    • B32B17/10Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin
    • B32B17/10005Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing
    • B32B17/1055Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing characterized by the resin layer, i.e. interlayer
    • B32B17/10798Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing characterized by the resin layer, i.e. interlayer containing silicone
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00Layered products comprising a layer of synthetic resin
    • B32B27/06Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material
    • B32B27/08Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00Layered products comprising a layer of synthetic resin
    • B32B27/18Layered products comprising a layer of synthetic resin characterised by the use of special additives
    • B32B27/22Layered products comprising a layer of synthetic resin characterised by the use of special additives using plasticisers
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B7/00Layered products characterised by the relation between layers; Layered products characterised by the relative orientation of features between layers, or by the relative values of a measurable parameter between layers, i.e. products comprising layers having different physical, chemical or physicochemical properties; Layered products characterised by the interconnection of layers
    • B32B7/02Physical, chemical or physicochemical properties
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B60VEHICLES IN GENERAL
    • B60JWINDOWS, WINDSCREENS, NON-FIXED ROOFS, DOORS, OR SIMILAR DEVICES FOR VEHICLES; REMOVABLE EXTERNAL PROTECTIVE COVERINGS SPECIALLY ADAPTED FOR VEHICLES
    • B60J1/00Windows; Windscreens; Accessories therefor
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2307/00Properties of the layers or laminate
    • B32B2307/40Properties of the layers or laminate having particular optical properties
    • B32B2307/418Refractive
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2419/00Buildings or parts thereof
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2605/00Vehicles
    • B32B2605/006Transparent parts other than made from inorganic glass, e.g. polycarbonate glazings

Definitions

  • the present invention relates to an interlayer film for laminated glass used for obtaining laminated glass. Moreover, this invention relates to the laminated glass using the said intermediate film for laminated glasses.
  • Laminated glass is superior in safety even if it is damaged by an external impact and the amount of glass fragments scattered is small. For this reason, the said laminated glass is widely used for a motor vehicle, a rail vehicle, an aircraft, a ship, a building, etc.
  • the laminated glass is manufactured by sandwiching an interlayer film for laminated glass between two glass plates.
  • the interlayer film for laminated glass includes a single-layer interlayer film having a single-layer structure and a multilayer interlayer film having a structure of two or more layers.
  • Patent Document 1 As an example of the interlayer film for laminated glass, Patent Document 1 listed below discloses that 100 parts by weight of a polyvinyl acetal resin having a degree of acetalization of 60 to 85 mol% and at least one of alkali metal salts and alkaline earth metal salts. A sound insulating layer containing 0.001 to 1.0 parts by weight of a metal salt of the above and a plasticizer exceeding 30 parts by weight is disclosed. This sound insulation layer may be a single layer and used as an intermediate film.
  • Patent Document 1 also describes a multilayer intermediate film in which the sound insulation layer and other layers are laminated.
  • the other layer laminated on the sound insulation layer is composed of 100 parts by weight of a polyvinyl acetal resin having an acetalization degree of 60 to 85 mol%, and at least one metal salt of at least one of an alkali metal salt and an alkaline earth metal salt. 1.0 part by weight and a plasticizer that is 30 parts by weight or less are included.
  • Patent Document 2 discloses an intermediate film which is a polymer layer having a glass transition temperature of 33 ° C. or higher. Patent Document 2 describes that the polymer layer is disposed between glass plates having a thickness of 4.0 mm or less.
  • the plasticizer migrates from the layer having a high plasticizer content to the layer having a small plasticizer content, and the plasticizer bleeds on the surface of the interlayer film or the interface between the layers. May be out.
  • the elastic modulus of the intermediate film may change, the adhesiveness of the intermediate film may decrease, or the sound insulation of the laminated glass may decrease.
  • the present invention comprises a first layer and a second layer disposed on the first surface side of the first layer, the first layer comprising a polyvinyl acetal resin, A second resin component, the second layer contains a polyvinyl acetal resin, and the peak temperature of the loss tangent exhibited by the second resin component in the first layer is ⁇ 30 ° C. or higher and 10 ° C.
  • An interlayer film for laminated glass is provided, wherein the refractive index of the second resin component in the first layer is 1.47 or more and 1.51 or less.
  • the total amount of the polyvinyl acetal resin in the first layer and the second resin component in the first layer is 100% by weight.
  • the content of the polyvinyl acetal resin in one layer is 5% by weight or more and 60% by weight or less, and the content of the second resin component in the first layer is 40% by weight or more and 95% by weight or less. is there.
  • the weight average molecular weight of the second resin component in the first layer is 10,000 or more and 500,000 or less.
  • the absolute difference in refractive index between the polyvinyl acetal resin in the first layer and the second resin component in the first layer is 0.003 or less.
  • the second resin component in the first layer is a resin different from the polyvinyl acetal resin.
  • the second resin component in the first layer is an acrylic polymer, a urethane polymer, a silicone polymer, a rubber, or a vinyl acetate polymer. It is.
  • the second resin component in the first layer is an acrylic polymer.
  • the said intermediate film for laminated glasses is the 3rd arrange
  • the third layer includes a polyvinyl acetal resin.
  • the second layer includes a plasticizer
  • the third layer includes a plasticizer
  • the first laminated glass member, the second laminated glass member, and the interlayer film for laminated glass described above are provided, and the first laminated glass member and the second laminated glass are provided.
  • the interlayer film for laminated glass according to the present invention includes a first layer and a second layer disposed on the first surface side of the first layer, and the first layer is a polyvinyl acetal resin.
  • the second resin component, the second layer contains a polyvinyl acetal resin, and the peak temperature of loss tangent exhibited by the second resin component in the first layer is ⁇ 30 ° C. or higher, 10 ° C. or lower, and the refractive index of the second resin component in the first layer is 1.47 or more and 1.51 or less, so that the rigidity of the laminated glass using the intermediate film can be increased.
  • the sound insulation of the laminated glass can be enhanced and the recyclability can be enhanced.
  • FIG. 1 is a cross-sectional view schematically showing an interlayer film for laminated glass according to the first embodiment of the present invention.
  • FIG. 2 is a cross-sectional view schematically showing an example of a laminated glass using the laminated glass interlayer film shown in FIG.
  • FIG. 3 is a schematic diagram for explaining a method for measuring the bending stiffness.
  • interlayer film for laminated glass The interlayer film for laminated glass according to the present invention (in this specification, sometimes abbreviated as “intermediate film”) has a structure of two or more layers.
  • the intermediate film according to the present invention includes a first layer and a second layer disposed on the surface side of the first layer.
  • the first layer includes a polyvinyl acetal resin and a second resin component.
  • the second layer includes a polyvinyl acetal resin.
  • the peak temperature of the loss tangent exhibited by the second resin component in the first layer is ⁇ 30 ° C. or higher and 10 ° C. or lower.
  • the refractive index of the second resin component in the first layer is 1.47 or more and 1.51 or less.
  • the interlayer film according to the present invention has the above-described configuration, the rigidity of the laminated glass using the interlayer film can be increased, and the penetration resistance of the laminated glass can be increased. Moreover, in order to obtain a laminated glass, an intermediate film is arrange
  • the laminated glass can be reduced in weight.
  • the laminated glass is lightweight, the amount of material used for the laminated glass can be reduced, and the environmental load can be reduced.
  • fuel efficiency can be improved, and as a result, environmental load can be reduced.
  • the laminated glass can be reduced in weight.
  • the rigidity of the laminated glass can be considerably increased by using the interlayer film according to the present invention.
  • the sound insulation can be improved, and the peak frequency of the loss coefficient can be easily controlled within a suitable range.
  • the peak frequency of the loss coefficient can be controlled in the range of 3000 to 8000 Hz, and can be controlled to 4000 Hz or higher.
  • the recovered material (collected intermediate film) used at least once to obtain the intermediate film may be reused.
  • the recovered material (collected intermediate film) used at least once to obtain the intermediate film includes unnecessary portions (ears) at both ends of the intermediate film generated in the intermediate film manufacturing process, and intermediate generated in the laminated glass manufacturing process.
  • An interlayer film obtained by separating and removing the glass plate from the laminated glass obtained by dismantling the constructed building can be used.
  • the unnecessary intermediate film generated in the intermediate film manufacturing process also corresponds to the recovered material used at least once to obtain the intermediate film.
  • the interlayer film material can be reused. In the present invention, haze after re-kneading can be lowered, and recyclability can be improved.
  • the intermediate film may have a two-layer structure or may have a structure of three or more layers, and includes a third layer in addition to the first layer and the second layer. It may be.
  • the intermediate film preferably includes a third layer disposed on the second surface side opposite to the first surface of the first layer.
  • FIG. 1 is a cross-sectional view schematically showing an interlayer film for laminated glass according to the first embodiment of the present invention.
  • the intermediate film 11 shown in FIG. 1 is a multilayer intermediate film having a structure of two or more layers.
  • the intermediate film 11 is used to obtain a laminated glass.
  • the intermediate film 11 is an intermediate film for laminated glass.
  • the intermediate film 11 includes a first layer 1, a second layer 2, and a third layer 3.
  • On the first surface 1a of the first layer 1, the second layer 2 is disposed and laminated.
  • the third layer 3 is disposed on the second surface 1b opposite to the first surface 1a of the first layer 1 and laminated.
  • the first layer 1 is an intermediate layer.
  • Each of the second layer 2 and the third layer 3 is a protective layer, and is a surface layer in the present embodiment.
  • the first layer 1 is arranged between the second layer 2 and the third layer 3 and is sandwiched between them. Therefore, the intermediate film 11 has a multilayer structure (second layer 2 / first layer 1 / third layer) in which the second layer 2, the first layer 1, and the third layer 3 are laminated in this order. Having layer
  • layers may be disposed between the second layer 2 and the first layer 1 and between the first layer 1 and the third layer 3, respectively.
  • the second layer 2 and the first layer 1 and the first layer 1 and the third layer 3 are preferably laminated directly.
  • examples of other layers include layers containing polyethylene terephthalate and the like.
  • the first layer 1 includes a polyvinyl acetal resin and a second resin component.
  • the second layer 2 includes a polyvinyl acetal resin.
  • the third layer 3 preferably contains a polyvinyl acetal resin.
  • the first layer includes a polyvinyl acetal resin (hereinafter sometimes referred to as a polyvinyl acetal resin (1)).
  • the second layer contains a polyvinyl acetal resin (hereinafter may be referred to as a polyvinyl acetal resin (2)).
  • the third layer preferably contains a polyvinyl acetal resin (hereinafter sometimes referred to as a polyvinyl acetal resin (3)).
  • the polyvinyl acetal resin (1), the polyvinyl acetal resin (2), and the polyvinyl acetal resin (3) may be the same or different.
  • the polyvinyl acetal resin (1) As for the said polyvinyl acetal resin (1), the said polyvinyl acetal resin (2), and the said polyvinyl acetal resin (3), only 1 type may respectively be used and 2 or more types may be used together.
  • the polyvinyl acetal resin includes an acetoacetalized resin.
  • the polyvinyl acetal resin can be produced, for example, by acetalizing polyvinyl alcohol with an aldehyde.
  • the polyvinyl acetal resin is preferably an acetalized product of polyvinyl alcohol.
  • the polyvinyl alcohol can be obtained, for example, by saponifying polyvinyl acetate.
  • the saponification degree of the polyvinyl alcohol is generally 70 to 99.9 mol%.
  • the average degree of polymerization of the polyvinyl alcohol is preferably 200 or more, more preferably 500 or more, still more preferably 1500 or more, still more preferably 1600 or more, particularly preferably 2600 or more, most preferably 2700 or more, preferably 5000 or less, More preferably, it is 4000 or less, More preferably, it is 3500 or less.
  • the average degree of polymerization is not less than the above lower limit, the penetration resistance of the laminated glass is further enhanced.
  • the average degree of polymerization is not more than the above upper limit, the intermediate film can be easily molded.
  • the average degree of polymerization of the polyvinyl alcohol is determined by a method based on JIS K6726 “Testing method for polyvinyl alcohol”.
  • the carbon number of the acetal group in the polyvinyl acetal resin is preferably 2 to 5, and preferably 2, 3 or 4. When the carbon number of the acetal group in the polyvinyl acetal resin is 3 or more, the glass transition temperature of the intermediate film is sufficiently low.
  • the carbon number of the acetal group in the polyvinyl acetal resin is preferably 2 or 4, and in this case, the production of the polyvinyl acetal resin is efficient.
  • an aldehyde having 1 to 10 carbon atoms is preferably used as the aldehyde.
  • the aldehyde having 1 to 10 carbon atoms include formaldehyde, acetaldehyde, propionaldehyde, n-butyraldehyde, isobutyraldehyde, n-valeraldehyde, 2-ethylbutyraldehyde, n-hexylaldehyde, n-octylaldehyde, Examples include n-nonyl aldehyde, n-decyl aldehyde, and benzaldehyde.
  • acetaldehyde, propionaldehyde, n-butyraldehyde, isobutyraldehyde, n-hexylaldehyde or n-valeraldehyde is preferable
  • acetaldehyde, propionaldehyde, n-butyraldehyde or isobutyraldehyde is more preferable
  • acetaldehyde, propionaldehyde or n More preferred is butyraldehyde.
  • the said aldehyde only 1 type may be used and 2 or more types may be used together.
  • the hydroxyl group content (hydroxyl group amount) of the polyvinyl acetal resin (1) is preferably 17 mol% or more, more preferably 20 mol% or more, still more preferably 22 mol% or more, preferably 40 mol% or less, more preferably. Is less than 35 mol%, more preferably 30 mol% or less, particularly preferably 25 mol% or less.
  • the hydroxyl group content is at least the above lower limit, the adhesive strength of the interlayer film is further increased.
  • the hydroxyl group content of the polyvinyl acetal resin (1) is 20 mol% or more, the reaction efficiency is high and the productivity is excellent, and when it is less than 35 mol%, the sound insulation of the laminated glass is further enhanced.
  • the hydroxyl group content is not more than the above upper limit, the flexibility of the interlayer film is increased, and the handling of the interlayer film is facilitated.
  • the content of each hydroxyl group in the polyvinyl acetal resin (2) and the polyvinyl acetal resin (3) is preferably 25 mol% or more, preferably 38 mol% or less, more preferably 35 mol% or less, still more preferably 32 mol%. % Or less, particularly preferably 30 mol% or less, and most preferably 27.5 mol% or less.
  • the hydroxyl group content is at least the above lower limit, the adhesive strength of the interlayer film is further increased.
  • the hydroxyl group content is not more than the above upper limit, the flexibility of the interlayer film is increased, and the handling of the interlayer film is facilitated. Moreover, rigidity becomes high effectively that the content rate of the said hydroxyl group is below the said upper limit.
  • the hydroxyl group content of the polyvinyl acetal resin is a value indicating the mole fraction obtained by dividing the amount of ethylene groups to which the hydroxyl group is bonded by the total amount of ethylene groups in the main chain, as a percentage.
  • the amount of the ethylene group to which the hydroxyl group is bonded can be measured, for example, according to JIS K6728 “Testing method for polyvinyl butyral”.
  • the degree of acetylation (acetyl group amount) of the polyvinyl acetal resin (1) is preferably 0.01 mol% or more, more preferably 0.1 mol% or more, still more preferably 7 mol% or more, still more preferably 9 It is at least mol%, preferably at most 30 mol%, more preferably at most 25 mol%, still more preferably at most 15 mol%.
  • the degree of acetylation is not less than the above lower limit, sound insulation is increased and compatibility between the polyvinyl acetal resin and the plasticizer is increased.
  • the acetylation degree is not more than the above upper limit, the moisture resistance of the interlayer film and the laminated glass is increased.
  • the degree of acetylation of the polyvinyl acetal resin (1) is 0.1 mol% or more and 25 mol% or less, the penetration resistance is excellent.
  • Each degree of acetylation of the polyvinyl acetal resin (2) and the polyvinyl acetal resin (3) is preferably 0.01 mol% or more, more preferably 0.5 mol% or more, preferably 10 mol% or less, more preferably. Is 2 mol% or less.
  • the acetylation degree is not less than the above lower limit, the compatibility between the polyvinyl acetal resin and the plasticizer is increased.
  • the acetylation degree is not more than the above upper limit, the moisture resistance of the interlayer film and the laminated glass is increased.
  • the degree of acetylation is a value obtained by dividing the amount of ethylene groups to which the acetyl group is bonded by the total amount of ethylene groups in the main chain, as a percentage.
  • the amount of ethylene group to which the acetyl group is bonded can be measured, for example, according to JIS K6728 “Testing method for polyvinyl butyral”.
  • the degree of acetalization of the polyvinyl acetal resin (1) is preferably 47 mol% or more, more preferably 60 mol% or more, preferably 80 mol% or less, more preferably It is 70 mol% or less.
  • the degree of acetalization is not less than the above lower limit, the interaction with the second resin component is increased, the toughness is increased, and the compatibility between the polyvinyl acetal resin and the plasticizer is increased.
  • the degree of acetalization is less than or equal to the above upper limit, the reaction time required for producing a polyvinyl acetal resin is shortened.
  • the degree of acetalization (degree of butyralization in the case of polyvinyl butyral resin) of the polyvinyl acetal resin (2) and the polyvinyl acetal resin (3) is preferably 55 mol% or more, more preferably 67 mol% or more, preferably Is 75 mol% or less, more preferably 71 mol% or less.
  • degree of acetalization is not less than the above lower limit, the compatibility between the polyvinyl acetal resin and the plasticizer increases.
  • the degree of acetalization is less than or equal to the above upper limit, the reaction time required for producing a polyvinyl acetal resin is shortened.
  • the degree of acetalization is the value obtained by subtracting the amount of ethylene groups bonded with hydroxyl groups and the amount of ethylene groups bonded with acetyl groups from the total amount of ethylene groups of the main chain. It is a value indicating the mole fraction obtained by dividing by the percentage.
  • the hydroxyl group content (hydroxyl content), acetalization degree (butyralization degree), and acetylation degree are preferably calculated from results measured by a method in accordance with JIS K6728 “Testing methods for polyvinyl butyral”. However, measurement by ASTM D1396-92 may be used.
  • the polyvinyl acetal resin is a polyvinyl butyral resin
  • the hydroxyl group content (hydroxyl amount), the acetalization degree (butyralization degree), and the acetylation degree are determined in accordance with JIS K6728 “Testing methods for polyvinyl butyral”. It can be calculated from the results measured by
  • the polyvinyl acetal resin (1) has an acetylation degree (a) of 8 mol% or less and an acetalization degree (a) of 65 mol%.
  • the polyvinyl acetal resin (A) as described above is preferable, or the polyvinyl acetal resin (B) having a degree of acetylation (b) exceeding 8 mol% is preferable.
  • the polyvinyl acetal resin (2) and the polyvinyl acetal resin (3) may be the polyvinyl acetal resin (A) or the polyvinyl acetal resin (B).
  • the degree of acetylation (a) of the polyvinyl acetal resin (A) is 8 mol% or less, preferably 7.5 mol% or less, more preferably 7 mol% or less, still more preferably 6.5 mol% or less, particularly preferably. It is 5 mol% or less, preferably 0.1 mol% or more, more preferably 0.5 mol% or more, still more preferably 0.8 mol% or more, and particularly preferably 1 mol% or more.
  • the degree of acetylation (a) is not more than the above upper limit and not less than the above lower limit, the migration of the plasticizer can be easily controlled, and the sound insulation of the laminated glass is further enhanced.
  • the degree of acetalization (a) of the polyvinyl acetal resin (A) is 65 mol% or more, preferably 67 mol% or more, more preferably 70 mol% or more, still more preferably 70.5 mol% or more, and further preferably 71. Mol% or more, still more preferably 71.5 mol% or more, particularly preferably 72 mol% or more, preferably 85 mol% or less, more preferably 83 mol% or less, still more preferably 81 mol% or less, particularly preferably 79. It is less than mol%.
  • the acetalization degree (a) is not less than the above lower limit, the sound insulating properties of the laminated glass are further enhanced.
  • the reaction time required in order to manufacture polyvinyl acetal resin (A) as the said acetalization degree (a) is below the said upper limit can be shortened.
  • the content (a) of the hydroxyl group in the polyvinyl acetal resin (A) is preferably 18 mol% or more, more preferably 19 mol% or more, still more preferably 20 mol% or more, particularly preferably 21 mol% or more, preferably 40 Mol% or less, more preferably 37 mol% or less, even more preferably 34 mol% or less, still more preferably 31 mol% or less, still more preferably 30 mol% or less, particularly preferably 29 mol% or less, and most preferably 28 mol% or less. It is less than mol%.
  • the hydroxyl group content (a) is not less than the above lower limit, the adhesive strength of the first layer is further increased.
  • the hydroxyl group content (a) is not more than the above upper limit, the sound insulation of the laminated glass is further enhanced.
  • the degree of acetylation (b) of the polyvinyl acetal resin (B) exceeds 8 mol%, preferably 9 mol% or more, more preferably 9.5 mol% or more, still more preferably 10 mol% or more, particularly preferably. 10.5 mol% or more, preferably 30 mol% or less, more preferably 28 mol% or less, still more preferably 26 mol% or less, and particularly preferably 24 mol% or less.
  • the acetylation degree (b) is not less than the above lower limit, the sound insulation of the laminated glass is further enhanced.
  • the reaction time required in order to manufacture polyvinyl acetal resin (B) as the said acetylation degree (b) is below the said upper limit can be shortened.
  • the degree of acetalization (b) of the polyvinyl acetal resin (B) is preferably 50 mol% or more, more preferably 53 mol% or more, still more preferably 55 mol% or more, particularly preferably 60 mol% or more, preferably 80 mol%. % Or less, more preferably 78 mol% or less, still more preferably 76 mol% or less, and particularly preferably 74 mol% or less.
  • the acetalization degree (b) is not less than the above lower limit, the sound insulating properties of the laminated glass are further enhanced.
  • the reaction time required in order to manufacture polyvinyl acetal resin (B) as the said acetalization degree (b) is below the said upper limit can be shortened.
  • the hydroxyl group content (b) of the polyvinyl acetal resin (B) is preferably 18 mol% or more, more preferably 19 mol% or more, still more preferably 20 mol% or more, particularly preferably 21 mol% or more, preferably 38. It is not more than mol%, more preferably not more than 35 mol%, still more preferably not more than 31 mol%, still more preferably not more than 30 mol%, still more preferably not more than 29 mol%, particularly preferably not more than 28 mol%.
  • the hydroxyl group content (b) is not less than the above lower limit, the adhesive strength of the second layer is further increased.
  • the hydroxyl group content (b) is not more than the above upper limit, the sound insulating properties of the laminated glass are further enhanced.
  • the polyvinyl acetal resin (A) and the polyvinyl acetal resin (B) are each preferably a polyvinyl butyral resin, a polyvinyl acetoacetal resin, or a polyvinyl butyral-polyvinyl acetoacetal resin (co-acetal resin). It is more preferable that
  • the first layer includes a second resin component in addition to the polynyl acetal resin.
  • the second resin component is preferably not compatible with the polyvinyl acetal resin in the first layer because it is more excellent due to the effects of the present invention.
  • the second layer may contain the second resin component.
  • the third layer may contain the second resin component. As for the said 2nd resin component, only 1 type may be used and 2 or more types may be used together.
  • the second resin component in the first layer is different from the polyvinyl acetal resin. It is preferable that
  • the second resin component is an acrylic polymer, urethane polymer, silicone polymer, rubber.
  • a vinyl acetate polymer more preferably an acrylic polymer or a vinyl acetate polymer, and still more preferably an acrylic polymer.
  • the polymer includes a copolymer.
  • the acrylic polymer should be a polymer of a polymerization component containing a (meth) acrylic acid ester. Is preferred. By selecting the kind and blending amount of (meth) acrylic acid ester, the glass transition temperature of the second resin component can be easily controlled.
  • the peak temperature of loss tangent of the second resin component in the first layer is ⁇ 30 ° C. or higher and 10 ° C. or lower.
  • the peak temperature of the loss tangent of the second resin component in the first layer is ⁇ 15 ° C. or higher, more preferably ⁇ 10 ° C. or higher, and further preferably ⁇ 7 ° C. or higher because it is more excellent due to the effect of the present invention.
  • the temperature is preferably 3 ° C. or lower.
  • the absolute value of the difference in refractive index between the polyvinyl acetal resin in the first layer and the second resin component in the first layer is: Preferably it is 0.004 or less, More preferably, it is 0.003 or less, More preferably, it is 0.0025 or less.
  • the refractive index of the second resin component in the first layer is 1.47 or more and 1.51 or less. From the viewpoint of improving the rigidity and sound insulation with a good balance, the refractive index of the second resin component in the first layer is 1.475 or more, preferably 1.5 or less.
  • the weight average molecular weight of the second resin component is preferably 8000 or more, more preferably 10,000 or more. More preferably, it is 30000 or more, preferably 1000000 or less, more preferably 800000 or less, and further preferably 500000 or less.
  • the said weight average molecular weight shows the molecular weight in polystyrene conversion calculated
  • the second resin component may be interspersed in the polyvinyl acetal resin, and the polyvinyl acetal resin may be interspersed in the second resin component. .
  • the polyvinyl acetal resin and the second resin component may form a sea-island structure.
  • the polyvinyl acetal resin may be a sea part, and the second resin component may be an island part, the second resin component may be a sea part, and the polyvinyl acetal resin may be an island part.
  • the polyvinyl acetal resin may be continuous (may have a continuous structure), and the second resin component may be continuous (have a continuous structure).
  • the polyvinyl acetal resin and the second resin component may form a co-continuous structure.
  • the polyvinyl acetal resin may be present in a network form
  • the second resin component may be present in a network form.
  • the polyvinyl acetal resin and the second resin component preferably have a sea-island structure or a co-continuous structure, and the polyvinyl acetal resin and the second resin component have a sea-island structure.
  • the first layer has a sea-island structure with the polyvinyl acetal resin and the second resin component.
  • a sea-island structure in which the polyvinyl acetal resin constitutes the sea is preferable.
  • the average diameter of the islands is preferably 15 nm or more, more preferably 20 nm or more, still more preferably 30 nm or more, preferably 13 ⁇ m or less, more preferably 10 ⁇ m or less, and even more preferably 2 ⁇ m or less.
  • the diameter of one island part indicates the maximum diameter, and the average of the island parts is obtained by averaging the diameters (maximum diameters) of a plurality of islands.
  • the content of the polyvinyl acetal resin in the first layer is 5% by weight or more (preferably 10% by weight or more, more preferably 15% by weight or more), 60% by weight or less (preferably 55% by weight or less, more preferably 50% by weight or less), and the content of the skeleton derived from the second resin component in the copolymer in the first layer is 40% by weight or more (preferably 45% by weight or more, more preferably 50% by weight). Above), 95% by weight or less (preferably 90% by weight or less, more preferably 85% by weight or less).
  • the first layer does not contain or contains a plasticizer (hereinafter sometimes referred to as plasticizer (1)).
  • the first layer preferably contains a plasticizer (1).
  • the second layer preferably contains a plasticizer (hereinafter sometimes referred to as a plasticizer (2)).
  • the third layer preferably contains a plasticizer (hereinafter may be referred to as a plasticizer (3)).
  • plasticizer (1), the plasticizer (2), and the plasticizer (3) may be the same or different. As for the said plasticizer, only 1 type may be used and 2 or more types may be used together.
  • plasticizer examples include organic ester plasticizers such as monobasic organic acid esters and polybasic organic acid esters, and organic phosphate plasticizers such as organic phosphoric acid plasticizers and organic phosphorous acid plasticizers. . Of these, organic ester plasticizers are preferred.
  • the plasticizer is preferably a liquid plasticizer.
  • Examples of the monobasic organic acid ester include glycol esters obtained by a reaction between glycol and a monobasic organic acid.
  • Examples of the glycol include triethylene glycol, tetraethylene glycol, and tripropylene glycol.
  • Examples of the monobasic organic acid include butyric acid, isobutyric acid, caproic acid, 2-ethylbutyric acid, heptylic acid, n-octylic acid, 2-ethylhexylic acid, n-nonylic acid, and decylic acid.
  • polybasic organic acid ester examples include ester compounds of a polybasic organic acid and an alcohol having a linear or branched structure having 4 to 8 carbon atoms.
  • polybasic organic acid examples include adipic acid, sebacic acid, and azelaic acid.
  • organic ester plasticizer examples include triethylene glycol di-2-ethylpropanoate, triethylene glycol di-2-ethylbutyrate, triethylene glycol di-2-ethylhexanoate, triethylene glycol dicaprylate, Triethylene glycol di-n-octanoate, triethylene glycol di-n-heptanoate, tetraethylene glycol di-n-heptanoate, dibutyl sebacate, dioctyl azelate, dibutyl carbitol adipate, ethylene glycol di-2-ethylbutyrate, 1,3-propylene glycol di-2-ethyl butyrate, 1,4-butylene glycol di-2-ethyl butyrate, diethylene glycol di-2-ethyl butyrate, diethylene glycol di-2-ethyl Hexanoate, dipropylene glycol di-2-ethylbutyrate, triethylene glycol di-2-eth
  • organic phosphate plasticizer examples include tributoxyethyl phosphate, isodecylphenyl phosphate, triisopropyl phosphate, and the like.
  • the plasticizer is preferably a diester plasticizer represented by the following formula (1).
  • R1 and R2 each represent an organic group having 2 to 10 carbon atoms
  • R3 represents an ethylene group, an isopropylene group or an n-propylene group
  • p represents an integer of 3 to 10
  • R1 and R2 in the above formula (1) are each preferably an organic group having 5 to 10 carbon atoms, and more preferably an organic group having 6 to 10 carbon atoms.
  • the plasticizer preferably contains triethylene glycol di-2-ethylhexanoate (3GO), triethylene glycol di-2-ethylbutyrate (3GH) or triethylene glycol di-2-ethylpropanoate. More preferably, it contains triethylene glycol di-2-ethylhexanoate or triethylene glycol di-2-ethylbutyrate, and more preferably contains triethylene glycol di-2-ethylhexanoate.
  • 3GO triethylene glycol di-2-ethylhexanoate
  • GGH triethylene glycol di-2-ethylbutyrate
  • triethylene glycol di-2-ethylpropanoate More preferably, it contains triethylene glycol di-2-ethylhexanoate or triethylene glycol di-2-ethylbutyrate, and more preferably contains triethylene glycol di-2-ethylhexanoate.
  • Content of the plasticizer (2) with respect to 100 parts by weight of the polyvinyl acetal resin (2) (hereinafter sometimes referred to as content (2)), and plastic with respect to 100 parts by weight of the polyvinyl acetal resin (3)
  • the content of the agent (3) (hereinafter sometimes referred to as “content (3)”) is preferably 1 part by weight or more, more preferably 3 parts by weight or more, still more preferably 20 parts by weight or more, particularly preferably. Is 25 parts by weight or more, preferably 40 parts by weight or less, more preferably 35 parts by weight or less, still more preferably 32 parts by weight or less, and particularly preferably 30 parts by weight or less.
  • the flexibility of the intermediate film is increased and the handling of the intermediate film is facilitated.
  • the rigidity is effectively increased.
  • the content (2) and the content (3) are not more than the above upper limit, the mechanical strength of the interlayer film is further increased, and the penetration resistance of the laminated glass is further increased. In particular, when the content (2) and the content (3) are 35 parts by weight or less, the penetration resistance of the laminated glass is effectively increased.
  • the content of the plasticizer (1) (hereinafter sometimes referred to as content (1)) with respect to a total of 100 parts by weight of the polyvinyl acetal resin (1) and the second resin component is preferably 0 weight. Part (unused) or more, more preferably 1 part by weight or more, further preferably 3 parts by weight or more, preferably 80 parts by weight or less, more preferably 70 parts by weight or less, still more preferably 50 parts by weight or less, particularly preferably 30 parts by weight. Less than parts by weight. Since the first layer contains the second resin component, it is not necessary to use a plasticizer, and even when a plasticizer is used, the content of the plasticizer can be reduced. Since the plasticizer is relatively expensive, the cost of the intermediate film can be reduced by reducing the amount of the plasticizer used.
  • the content (2) is preferably greater than the content (1), and the content (3) is greater than the content (1).
  • the absolute value of the difference between the content (2) and the content (1), the content (3), and the content (1) is preferably 2 parts by weight or more, more preferably 5 parts by weight or more, and still more preferably 8 parts by weight or more.
  • the absolute value of the difference between the content (2) and the content (1) and the absolute value of the difference between the content (3) and the content (1) are each preferably 40 parts by weight or less.
  • the intermediate film preferably contains a heat shielding compound.
  • the first layer preferably contains a heat shielding compound.
  • the second layer preferably contains a heat shielding compound.
  • the third layer preferably includes a heat shielding compound.
  • the said heat-shielding compound only 1 type may be used and 2 or more types may be used together.
  • the intermediate film preferably includes at least one component X among a phthalocyanine compound, a naphthalocyanine compound, and an anthracocyanine compound.
  • the first layer preferably contains the component X.
  • the second layer preferably contains the component X.
  • the third layer preferably contains the component X.
  • the component X is a heat shielding compound. As for the said component X, only 1 type may be used and 2 or more types may be used together.
  • the component X is not particularly limited.
  • component X conventionally known phthalocyanine compounds, naphthalocyanine compounds and anthracocyanine compounds can be used.
  • Examples of the component X include phthalocyanine, a derivative of phthalocyanine, naphthalocyanine, a derivative of naphthalocyanine, an anthocyanin, and an anthocyanin derivative.
  • the phthalocyanine compound and the phthalocyanine derivative preferably each have a phthalocyanine skeleton.
  • the naphthalocyanine compound and the naphthalocyanine derivative preferably each have a naphthalocyanine skeleton. It is preferable that each of the anthocyanin compound and the derivative of the anthracyanine has an anthracyanine skeleton.
  • the component X is preferably at least one selected from the group consisting of phthalocyanine, phthalocyanine derivatives, naphthalocyanine, and naphthalocyanine derivatives. More preferably, it is at least one of phthalocyanine and phthalocyanine derivatives.
  • the component X preferably contains a vanadium atom or a copper atom.
  • the component X preferably contains a vanadium atom, and preferably contains a copper atom.
  • the component X is more preferably at least one of a phthalocyanine containing a vanadium atom or a copper atom and a phthalocyanine derivative containing a vanadium atom or a copper atom.
  • the component X preferably has a structural unit in which an oxygen atom is bonded to a vanadium atom.
  • the content of the component X is preferably 0.001% by weight or more, more preferably 0.005. % By weight or more, more preferably 0.01% by weight or more, particularly preferably 0.02% by weight or more, preferably 0.2% by weight or less, more preferably 0.1% by weight or less, still more preferably 0.05% by weight. % Or less, particularly preferably 0.04% by weight or less.
  • the content of the component X is not less than the above lower limit and not more than the above upper limit, the heat shielding property is sufficiently high and the visible light transmittance is sufficiently high.
  • the visible light transmittance can be 70% or more.
  • Thermal barrier particles The intermediate film preferably contains heat shielding particles.
  • the first layer preferably contains the heat shielding particles.
  • the second layer preferably includes the heat shielding particles.
  • the third layer preferably contains the heat shielding particles.
  • the heat shielding particles are heat shielding compounds. By using heat shielding particles, infrared rays (heat rays) can be effectively blocked. As for the said heat-shielding particle, only 1 type may be used and 2 or more types may be used together.
  • the heat shielding particles are more preferably metal oxide particles.
  • the heat shielding particles are preferably particles (metal oxide particles) formed of a metal oxide.
  • Infrared rays having a wavelength longer than 780 nm longer than visible light have a smaller amount of energy than ultraviolet rays.
  • infrared rays have a large thermal effect, and when infrared rays are absorbed by a substance, they are released as heat. For this reason, infrared rays are generally called heat rays.
  • heat shielding particles By using the heat shielding particles, infrared rays (heat rays) can be effectively blocked.
  • the heat shielding particles mean particles that can absorb infrared rays.
  • heat shielding particles include aluminum-doped tin oxide particles, indium-doped tin oxide particles, antimony-doped tin oxide particles (ATO particles), gallium-doped zinc oxide particles (GZO particles), and indium-doped zinc oxide particles (IZO particles).
  • Aluminum doped zinc oxide particles (AZO particles), niobium doped titanium oxide particles, sodium doped tungsten oxide particles, cesium doped tungsten oxide particles, thallium doped tungsten oxide particles, rubidium doped tungsten oxide particles, tin doped indium oxide particles (ITO particles) And metal oxide particles such as tin-doped zinc oxide particles and silicon-doped zinc oxide particles, and lanthanum hexaboride (LaB 6 ) particles. Heat shielding particles other than these may be used.
  • metal oxide particles are preferable because of their high heat ray shielding function, ATO particles, GZO particles, IZO particles, ITO particles or tungsten oxide particles are more preferable, and ITO particles or tungsten oxide particles are particularly preferable.
  • tin-doped indium oxide particles ITO particles
  • tungsten oxide particles are also preferable because they have a high heat ray shielding function and are easily available.
  • the tungsten oxide particles are generally represented by the following formula (X1) or the following formula (X2).
  • tungsten oxide particles represented by the following formula (X1) or the following formula (X2) are preferably used.
  • W represents tungsten
  • O represents oxygen
  • y and z satisfy 2.0 ⁇ z / y ⁇ 3.0.
  • M is H, He, alkali metal, alkaline earth metal, rare earth element, Mg, Zr, Cr, Mn, Fe, Ru, Co, Rh, Ir, Ni, Pd, Pt, Cu , Ag, Au, Zn, Cd, Al, Ga, In, Tl, Si, Ge, Sn, Pb, Sb, B, F, P, S, Se, Br, Te, Ti, Nb, V, Mo, Ta
  • O represents oxygen
  • x, y, and z represent 0.001 ⁇ x / y ⁇ 1, and 2.0 ⁇ z / y ⁇ 3.0 is satisfied.
  • the tungsten oxide particles are preferably metal-doped tungsten oxide particles.
  • the “tungsten oxide particles” include metal-doped tungsten oxide particles. Specific examples of the metal-doped tungsten oxide particles include sodium-doped tungsten oxide particles, cesium-doped tungsten oxide particles, thallium-doped tungsten oxide particles, and rubidium-doped tungsten oxide particles.
  • cesium-doped tungsten oxide particles are particularly preferable.
  • the cesium-doped tungsten oxide particles are preferably tungsten oxide particles represented by the formula: Cs 0.33 WO 3 .
  • the average particle diameter of the heat shielding particles is preferably 0.01 ⁇ m or more, more preferably 0.02 ⁇ m or more, preferably 0.1 ⁇ m or less, more preferably 0.05 ⁇ m or less.
  • the average particle size is not less than the above lower limit, the heat ray shielding property is sufficiently increased.
  • the average particle size is not more than the above upper limit, the dispersibility of the heat shielding particles is increased.
  • the above “average particle diameter” indicates the volume average particle diameter.
  • the average particle diameter can be measured using a particle size distribution measuring device (“UPA-EX150” manufactured by Nikkiso Co., Ltd.) or the like.
  • the content of the heat shielding particles is preferably 0.01% by weight or more, more preferably 0%. 0.1% by weight or more, more preferably 1% by weight or more, particularly preferably 1.5% by weight or more, preferably 6% by weight or less, more preferably 5.5% by weight or less, still more preferably 4% by weight or less, Preferably it is 3.5 weight% or less, Most preferably, it is 3.0 weight% or less.
  • the content of the heat shielding particles is not less than the above lower limit and not more than the above upper limit, the heat shielding property is sufficiently high and the visible light transmittance is sufficiently high.
  • the layer (the first layer, the second layer, or the third layer) containing the heat shielding particles may contain the heat shielding particles at a ratio of 0.1 g / m 2 or more and 12 g / m 2 or less. preferable. When the ratio of the heat shielding particles is within the above range, the heat shielding property is sufficiently high and the visible light transmittance is sufficiently high.
  • the proportion of the heat shielding particles is preferably 0.5 g / m 2 or more, more preferably 0.8 g / m 2 or more, still more preferably 1.5 g / m 2 or more, particularly preferably 3 g / m 2 or more, preferably Is 11 g / m 2 or less, more preferably 10 g / m 2 or less, still more preferably 9 g / m 2 or less, and particularly preferably 7 g / m 2 or less.
  • the ratio is equal to or higher than the lower limit, the heat shielding property is further enhanced.
  • the ratio is less than or equal to the upper limit, the visible light transmittance is further increased.
  • the intermediate film preferably contains at least one metal salt (hereinafter sometimes referred to as a metal salt M) of an alkali metal salt and an alkaline earth metal salt.
  • the first layer preferably includes the metal salt M.
  • the second layer preferably contains the metal salt M.
  • the third layer preferably contains the metal salt M.
  • Use of the metal salt M makes it easy to control the adhesion between the interlayer film and the laminated glass member or the adhesion between the layers in the interlayer film.
  • the said metal salt M only 1 type may be used and 2 or more types may be used together.
  • the metal salt M preferably contains at least one metal selected from the group consisting of Li, Na, K, Rb, Cs, Mg, Ca, Sr and Ba.
  • the metal salt contained in the interlayer film preferably contains at least one metal of K and Mg.
  • the metal salt M is more preferably an alkali metal salt of an organic acid having 2 to 16 carbon atoms or an alkaline earth metal salt of an organic acid having 2 to 16 carbon atoms, and a carboxylic acid having 2 to 16 carbon atoms. More preferably, it is a magnesium salt or a potassium salt of a carboxylic acid having 2 to 16 carbon atoms.
  • magnesium salt of carboxylic acid having 2 to 16 carbon atoms and the potassium salt of carboxylic acid having 2 to 16 carbon atoms include, but are not limited to, for example, magnesium acetate, potassium acetate, magnesium propionate, potassium propionate, 2-ethylbutyric acid
  • magnesium, potassium 2-ethylbutanoate, magnesium 2-ethylhexanoate and potassium 2-ethylhexanoate examples include magnesium, potassium 2-ethylbutanoate, magnesium 2-ethylhexanoate and potassium 2-ethylhexanoate.
  • the total content of Mg and K in the layer containing the metal salt M is preferably 5 ppm or more, more preferably 10 ppm or more, and even more preferably 20 ppm or more. , Preferably 300 ppm or less, more preferably 250 ppm or less, still more preferably 200 ppm or less.
  • the adhesion between the interlayer film and the laminated glass member or the adhesion between the layers in the interlayer film can be controlled even better.
  • the intermediate film preferably contains an ultraviolet shielding agent.
  • the first layer preferably contains an ultraviolet shielding agent.
  • the second layer preferably contains an ultraviolet shielding agent.
  • the third layer preferably contains an ultraviolet shielding agent.
  • the ultraviolet shielding agent includes an ultraviolet absorber.
  • the ultraviolet shielding agent is preferably an ultraviolet absorber.
  • the ultraviolet shielding agent examples include a metal-based ultraviolet shielding agent (a metal-containing ultraviolet shielding agent), a metal oxide-based ultraviolet shielding agent (an ultraviolet shielding agent containing a metal oxide), and a benzotriazole-based ultraviolet shielding agent ( UV shielding agent having a benzotriazole structure), benzophenone UV shielding agent (UV shielding agent having a benzophenone structure), triazine UV shielding agent (UV shielding agent having a triazine structure), malonic ester UV shielding agent (malonic acid) And an oxalic acid anilide type ultraviolet shielding agent (ultraviolet shielding agent having an oxalic acid anilide structure) and a benzoate type ultraviolet shielding agent (ultraviolet shielding agent having a benzoate structure).
  • a metal-based ultraviolet shielding agent a metal-containing ultraviolet shielding agent
  • a metal oxide-based ultraviolet shielding agent an ultraviolet shielding agent containing a metal oxide
  • the metallic ultraviolet shielding agent examples include platinum particles, particles in which the surface of the platinum particles is coated with silica, palladium particles, particles in which the surface of the palladium particles is coated with silica, and the like.
  • the ultraviolet shielding agent is preferably not a heat shielding particle.
  • the ultraviolet shielding agent is preferably a benzotriazole ultraviolet shielding agent, a benzophenone ultraviolet shielding agent, a triazine ultraviolet shielding agent or a benzoate ultraviolet shielding agent, more preferably a benzotriazole ultraviolet shielding agent or a benzophenone ultraviolet shielding agent. More preferably, it is a benzotriazole ultraviolet shielding agent.
  • metal oxide ultraviolet shielding agent examples include zinc oxide, titanium oxide, and cerium oxide. Furthermore, the surface of the metal oxide ultraviolet shielding agent may be coated. Examples of the coating material on the surface of the metal oxide ultraviolet shielding agent include insulating metal oxides, hydrolyzable organosilicon compounds, and silicone compounds.
  • the insulating metal oxide examples include silica, alumina and zirconia.
  • the insulating metal oxide has a band gap energy of 5.0 eV or more, for example.
  • benzotriazole ultraviolet shielding agent examples include 2- (2′-hydroxy-5′-methylphenyl) benzotriazole (“TinvinP” manufactured by BASF), 2- (2′-hydroxy-3 ′, 5 ′). -Di-t-butylphenyl) benzotriazole (“Tinvin 320” manufactured by BASF), 2- (2'-hydroxy-3'-t-butyl-5-methylphenyl) -5-chlorobenzotriazole (manufactured by BASF " And benzotriazole-based UV screening agents such as 2- (2′-hydroxy-3 ′, 5′-di-amylphenyl) benzotriazole (“Tinvin 328” manufactured by BASF)).
  • the ultraviolet shielding agent is preferably a benzotriazole-based ultraviolet shielding agent containing a halogen atom, and more preferably a benzotriazole-based ultraviolet shielding agent containing a chlorine atom, because of its excellent ability to absorb ultraviolet rays.
  • benzophenone-based ultraviolet shielding agent examples include octabenzone (“Chimasorb 81” manufactured by BASF).
  • triazine-based ultraviolet shielding agent examples include “LA-F70” manufactured by ADEKA and 2- (4,6-diphenyl-1,3,5-triazin-2-yl) -5-[(hexyl) oxy].
  • -Phenol Teuvin 1577FF manufactured by BASF
  • malonic ester-based ultraviolet shielding agent examples include 2- (p-methoxybenzylidene) malonic acid dimethyl, tetraethyl-2,2- (1,4-phenylenedimethylidene) bismalonate, 2- (p-methoxybenzylidene) -bis. (1,2,2,6,6-pentamethyl 4-piperidinyl) malonate and the like.
  • Hostavin B-CAP As commercial products of the above-mentioned malonic ester-based ultraviolet screening agents, there are Hostavin B-CAP, Hostavin PR-25, and Hostavin PR-31 (all manufactured by Clariant).
  • Examples of the oxalic acid anilide-based ultraviolet shielding agent include N- (2-ethylphenyl) -N ′-(2-ethoxy-5-tert-butylphenyl) oxalic acid diamide, N- (2-ethylphenyl) -N ′.
  • Oxalic acid diamides having an aryl group substituted on the nitrogen atom such as-(2-ethoxy-phenyl) oxalic acid diamide, 2-ethyl-2'-ethoxy-oxyanilide ("Sanduvor VSU" manufactured by Clariant) Can be mentioned.
  • benzoate ultraviolet shielding agent examples include 2,4-di-tert-butylphenyl-3,5-di-tert-butyl-4-hydroxybenzoate (“Tinuvin 120” manufactured by BASF).
  • the ultraviolet shielding is performed in 100% by weight of the layer containing the ultraviolet shielding agent (first layer, second layer, or third layer).
  • the content of the agent is preferably 0.1% by weight or more, more preferably 0.2% by weight or more, further preferably 0.3% by weight or more, particularly preferably 0.5% by weight or more, preferably 2.5%.
  • % By weight or less, more preferably 2% by weight or less, further preferably 1% by weight or less, and particularly preferably 0.8% by weight or less.
  • the content of the ultraviolet shielding agent is 0.2% by weight or more, thereby reducing the visible light transmittance after the lapse of the period of the interlayer film and the laminated glass. Remarkably suppressed.
  • the intermediate film preferably contains an antioxidant.
  • the first layer preferably contains an antioxidant.
  • the second layer preferably contains an antioxidant.
  • the third layer preferably contains an antioxidant. As for the said antioxidant, only 1 type may be used and 2 or more types may be used together.
  • antioxidants examples include phenol-based antioxidants, sulfur-based antioxidants, and phosphorus-based antioxidants.
  • the phenolic antioxidant is an antioxidant having a phenol skeleton.
  • the sulfur-based antioxidant is an antioxidant containing a sulfur atom.
  • the phosphorus antioxidant is an antioxidant containing a phosphorus atom.
  • the antioxidant is preferably a phenolic antioxidant or a phosphorus antioxidant.
  • phenolic antioxidant examples include 2,6-di-t-butyl-p-cresol (BHT), butylated hydroxyanisole (BHA), 2,6-di-t-butyl-4-ethylphenol, stearyl - ⁇ - (3,5-di-t-butyl-4-hydroxyphenyl) propionate, 2,2'-methylenebis- (4-methyl-6-butylphenol), 2,2'-methylenebis- (4-ethyl- 6-t-butylphenol), 4,4′-butylidene-bis- (3-methyl-6-t-butylphenol), 1,1,3-tris- (2-methyl-hydroxy-5-tert-butylphenyl) Butane, tetrakis [methylene-3- (3 ′, 5′-butyl-4-hydroxyphenyl) propionate] methane, 1,3,3-tris- (2-methyl-4- Droxy-5-tert-butylphenol) butane, 1,3,5-trimethyl-2,
  • Examples of the phosphorus antioxidant include tridecyl phosphite, tris (tridecyl) phosphite, triphenyl phosphite, trinonylphenyl phosphite, bis (tridecyl) pentaerythritol diphosphite, bis (decyl) pentaerythritol diphos.
  • antioxidants examples include “IRGANOX 245” manufactured by BASF, “IRGAFOS 168” manufactured by BASF, “IRGAFOS 38” manufactured by BASF, “Smilizer BHT” manufactured by Sumitomo Chemical, and “ IRGANOX 1010 ".
  • a layer in 100% by weight of the interlayer film or containing an antioxidant.
  • the content of the antioxidant is preferably 0.1% by weight or more.
  • the content of the antioxidant is preferably 2% by weight or less in 100% by weight of the intermediate film or 100% by weight of the layer containing the antioxidant.
  • the intermediate film, the first layer, the second layer, and the third layer may each include a flame retardant, an antistatic agent, a pigment, a dye, an adhesive force adjusting agent, a moisture resistant agent, a fluorescent enhancement agent, as necessary.
  • Additives such as whitening agents and infrared absorbers may be included. As for these additives, only 1 type may be used and 2 or more types may be used together.
  • the glass transition temperatures of the second layer and the third layer are preferably 31 ° C. or higher, more preferably 33 ° C. or higher, and still more preferably 35 ° C. or higher. It is.
  • the upper limit of the glass transition temperature of the second layer and the third layer is not particularly limited. From the viewpoint of further improving the sound insulation of the interlayer film, the glass transition temperature of the second layer and the third layer may be 60 ° C. or less.
  • the thickness of the intermediate film is not particularly limited. From the viewpoint of practical use and the viewpoint of sufficiently increasing the penetration resistance and rigidity of the laminated glass, the thickness of the interlayer film is preferably 0.1 mm or more, more preferably 0.25 mm or more, preferably 3 mm or less, more preferably. Is 1.5 mm or less. When the thickness of the interlayer film is not less than the above lower limit, the penetration resistance and rigidity of the laminated glass are increased. When the thickness of the interlayer film is not more than the above upper limit, the transparency of the interlayer film is further improved.
  • T is the thickness of the intermediate film.
  • the thickness of the first layer is preferably 0.0625T or more, more preferably 0.1T or more, preferably 0.375T or less, more preferably 0.25T or less.
  • the thicknesses of the second layer and the third layer are preferably 0.3125T or more, more preferably 0.375T or more, preferably 0.9375T or less, and more preferably 0.9T or less.
  • Each thickness of the second layer and the third layer may be 0.46875T or less, or 0.45T or less.
  • the rigidity of a laminated glass becomes still higher that each thickness of the said 2nd layer and said 3rd layer is more than the said minimum and below the said upper limit, and it can suppress the bleed-out of a plasticizer.
  • the total thickness of the second layer and the third layer is preferably 0.625 T or more, more preferably 0.75 T or more, preferably 0.9375 T or less, more preferably 0.9 T or less. Further, when the total thickness of the second layer and the third layer is not less than the above lower limit and not more than the above upper limit, the rigidity of the laminated glass is further increased, and bleed out of the plasticizer can be suppressed.
  • the method for producing the interlayer film according to the present invention is not particularly limited.
  • As the method for producing an intermediate film according to the present invention after forming each layer using each resin composition for forming each layer, for example, a method for laminating each obtained layer, and for forming each layer The method etc. which laminate
  • the same polyvinyl acetal resin is contained in the second layer and the third layer, and the second layer, the third layer, It is more preferable that the same polyvinyl acetal resin and the same plasticizer are included, and it is more preferable that the second layer and the third layer are formed of the same resin composition.
  • the intermediate film preferably has an uneven shape on at least one of the surfaces on both sides. More preferably, the intermediate film has a concavo-convex shape on both surfaces. It does not specifically limit as a method of forming said uneven
  • FIG. 2 is a cross-sectional view schematically showing an example of a laminated glass using the laminated glass interlayer film shown in FIG.
  • the intermediate film 11 is disposed between the first laminated glass member 21 and the second laminated glass member 22 and is sandwiched.
  • the first laminated glass member 21 is laminated on the first surface 11 a of the intermediate film 11.
  • a second laminated glass member 22 is laminated on the second surface 11 b opposite to the first surface 11 a of the intermediate film 11.
  • a first laminated glass member 21 is laminated on the outer surface 2 a of the second layer 2.
  • a second laminated glass member 22 is laminated on the outer surface 3 a of the third layer 3.
  • the laminated glass which concerns on this invention is equipped with the 1st laminated glass member, the 2nd laminated glass member, and the intermediate film, and this intermediate film is the intermediate film for laminated glasses which concerns on this invention. It is.
  • the interlayer film is disposed between the first laminated glass member and the second laminated glass member.
  • laminated glass member examples include a glass plate and a PET (polyethylene terephthalate) film.
  • Laminated glass includes not only laminated glass in which an intermediate film is sandwiched between two glass plates, but also laminated glass in which an intermediate film is sandwiched between a glass plate and a PET film or the like.
  • the laminated glass is a laminate including a glass plate, and preferably at least one glass plate is used.
  • the glass plate examples include inorganic glass and organic glass.
  • the inorganic glass examples include float plate glass, heat ray absorbing plate glass, heat ray reflecting plate glass, polished plate glass, mold plate glass, netted plate glass, and lined plate glass.
  • the organic glass is a synthetic resin glass substituted for inorganic glass.
  • the organic glass examples include polycarbonate plates and poly (meth) acrylic resin plates.
  • the poly (meth) acrylic resin plate examples include a polymethyl (meth) acrylate plate.
  • the thickness of the laminated glass member is preferably 1 mm or more, preferably 5 mm or less, more preferably 3 mm or less.
  • the thickness of the glass plate is preferably 0.5 mm or more, more preferably 0.7 mm or more, preferably 5 mm or less, more preferably 3 mm or less.
  • the thickness of the PET film is preferably 0.03 mm or more, and preferably 0.5 mm or less.
  • the use of the interlayer film according to the present invention makes it possible to maintain high rigidity of the laminated glass even if the laminated glass is thin.
  • the thickness of the laminated glass member is preferably 2 mm or less, more preferably 1.8 mm or less, still more preferably 1.6 mm or less, still more preferably 1.5 mm or less, still more preferably 1.4 mm or less, and much more.
  • the total thickness of the two glass plates and the total thickness of the two laminated glass members in the laminated glass are preferably Is 4 mm or less, more preferably 3.6 mm or less, even more preferably 3.2 mm or less, even more preferably 3 mm or less, even more preferably 2.8 mm or less, even more preferably 2.6 mm or less, and even more preferably It is 2.4 mm or less, more preferably 2.2 mm or less, still more preferably 2 mm or less, still more preferably 1.6 mm or less, and particularly preferably 1.4 mm or less.
  • the method for producing the laminated glass is not particularly limited.
  • the intermediate film is sandwiched between the first laminated glass member and the second laminated glass member, passed through a pressing roll, or put in a rubber bag and sucked under reduced pressure, and the first The air remaining between the laminated glass member, the second laminated glass member and the intermediate film is degassed. Thereafter, it is pre-adhered at about 70 to 110 ° C. to obtain a laminate.
  • the laminate is put in an autoclave or pressed and pressed at about 120 to 150 ° C. and a pressure of 1 to 1.5 MPa. In this way, a laminated glass can be obtained. You may laminate
  • the interlayer film and the laminated glass can be used for automobiles, railway vehicles, aircraft, ships, buildings, and the like.
  • the said intermediate film and the said laminated glass can be used besides these uses.
  • the interlayer film and the laminated glass are preferably a vehicle or architectural interlayer film and a laminated glass, and more preferably a vehicle interlayer film and a laminated glass.
  • the intermediate film and the laminated glass can be used for an automobile windshield, side glass, rear glass, roof glass, or the like.
  • the interlayer film and the laminated glass are suitably used for automobiles.
  • the interlayer film is used for obtaining laminated glass for automobiles.
  • Polyvinyl acetal resin Polyvinyl acetal resin (A): using n-butyraldehyde, average polymerization degree of polyvinyl alcohol (PVA) 1700, hydroxyl group content 30.6 mol%, acetylation degree 0.9 mol%, acetalization degree (butyralization) Degree) 68.5 mol%
  • the degree of acetalization degree of butyralization
  • the degree of acetylation degree of acetylation
  • the hydroxyl group content was measured by a method in accordance with JIS K6728 “Testing methods for polyvinyl butyral”.
  • ASTM D1396-92 the same numerical value as the method based on JIS K6728 “Testing method for polyvinyl butyral” was shown.
  • Acrylic polymer Acrylic polymer (C): Acrylic polymer obtained by polymerizing a polymerization component containing 75% by weight of ethyl acrylate and 25% by weight of benzyl acrylate
  • Tinuvin 326 (2- (2′-hydroxy-3′-tert-butyl-5-methylphenyl) -5-chlorobenzotriazole, “Tinuvin 326” manufactured by BASF)
  • Example 1 Preparation of a composition for forming the first layer: 100 parts by weight of the polyvinyl acetal resin (A), 300 parts by weight of the acrylic polymer (A), 0.2 parts by weight of the ultraviolet shielding agent (Tinvin 326), and 0.2 parts by weight of the antioxidant (BHT) are mixed. A composition for forming the first layer was obtained.
  • compositions for forming the second and third layers Mixing 100 parts by weight of polyvinyl acetal resin (A), 20 parts by weight of plasticizer (3GO), 0.2 parts by weight of UV shielding agent (Tinuvin 326), and 0.2 parts by weight of antioxidant (BHT), A composition for forming the second layer and the third layer was obtained.
  • Preparation of interlayer film The composition for forming the first layer and the composition for forming the second layer and the third layer are coextruded using a coextrusion machine, whereby the second layer (thickness) An intermediate film (thickness 760 ⁇ m) having a laminated structure of 330 ⁇ m) / first layer (thickness 100 ⁇ m) / third layer (thickness 330 ⁇ m) was produced.
  • Laminated glass production Two glass plates washed and dried (first laminated glass member and second laminated glass member, clear float glass, length 25 cm ⁇ width 10 cm ⁇ thickness 2.5 mm) were prepared. The obtained interlayer film was sandwiched between the two glass plates to obtain a laminate. The obtained laminate was put in a rubber bag and deaerated at a vacuum degree of 2660 Pa (20 torr) for 20 minutes. Thereafter, the laminate was vacuum-pressed while being deaerated while being further kept at 90 ° C. for 30 minutes in an autoclave. The laminated body preliminarily pressure-bonded in this manner was pressure-bonded for 20 minutes in an autoclave under conditions of 135 ° C. and a pressure of 1.2 MPa (12 kg / cm 2 ) to obtain a laminated glass.
  • Examples 2 to 20 and Comparative Examples 1 to 4 Type and amount of compounding component used in composition for forming first layer, type and amount of compounding component used in composition for forming second layer and third layer, first The thickness of the layer, the thickness of the second layer, the thickness of the third layer, the thickness of the first laminated glass member and the thickness of the second laminated glass member were set as shown in Tables 1 to 4 below. In the same manner as in Example 1, an interlayer film and a laminated glass were obtained. In all Examples and Comparative Examples, the same type of ultraviolet shielding agent and antioxidant as in Example 1 were blended in the same amount (0.2 parts by weight) as in Example 1. If the intermediate film cannot be produced by coextrusion, the first layer, the second layer, and the third layer are formed by the solution casting method or the hot press method, respectively, and then laminated, so that the intermediate film can be easily formed. was gotten.
  • Peak temperature of glass transition temperature / loss tangent A kneaded material having each composition of the first layer in Examples and Comparative Examples was prepared.
  • the obtained kneaded material was press-molded with a press molding machine to obtain a resin film A having a thickness of 0.35 mm.
  • the obtained resin film A was allowed to stand for 2 hours at 25 ° C. and a relative humidity of 30%. After standing for 2 hours, viscoelasticity was measured using “ARES-G2” manufactured by TAINSTRUMENTS.
  • As a jig a parallel plate having a diameter of 8 mm was used. The measurement was performed under the condition of decreasing the temperature from 100 ° C. to ⁇ 50 ° C.
  • the peak temperature of the loss tangent was defined as the glass transition temperature Tg (° C.).
  • the high temperature side peak was derived from the polyvinyl acetal resin, and the low temperature side peak was derived from the second resin component.
  • the obtained laminated glass was prepared.
  • the bending stiffness was evaluated by the test method schematically shown in FIG.
  • a measuring apparatus a universal material testing machine 5966 manufactured by Instron Japan Company Limited equipped with a static three-point bending test jig 2810 was used.
  • the measurement temperature is 20 ⁇ 3 ° C.
  • the distance D1 is 18 cm
  • the distance D2 is 25 cm
  • the glass is deformed in the direction of F at a displacement speed of 1 mm / min
  • a displacement of 1.5 mm is applied. Stress was measured and bending stiffness was calculated. The bending stiffness was determined according to the following criteria.
  • Tensile properties (rigidity) of the first layer at 25 ° C. and 40 ° C. A composition for forming a first layer having a thickness of about 400 ⁇ m was prepared, and a tensile test was performed at a tensile rate of 200 mm / min using an autograph (“AG-IS” manufactured by Shimadzu Corporation). The Young's modulus at 40 ° C. was evaluated. Tensile properties were determined according to the following criteria.
  • the laminated glass is vibrated with a vibration generator for vibration testing ("Vibrator G21-005D” manufactured by KENKEN Co., Ltd.).
  • the vibration spectrum was analyzed with an FFT spectrum analyzer ("FFT analyzer HP3582A" manufactured by Yokogawa Hured Packard).
  • FFT analyzer HP3582A manufactured by Yokogawa Hured Packard.
  • the peak frequency of the loss factor was obtained, and the loss factor of the laminated glass at 3000 Hz at 20 ° C. was further calculated.
  • the sound insulation was judged from the loss coefficient according to the following criteria. In addition, if the loss coefficient is 0.1 or more, the sound insulation is excellent, and if the loss coefficient is 0.2 or more, the sound insulation is further excellent.
  • Loss coefficient is 0.2 or more
  • Loss coefficient is 0.1 or more and less than 0.2
  • Loss coefficient is less than 0.1
  • Refractive index By measuring the polyvinyl acetal resin and the second resin component of the composition for forming the first layer with a refractometer (ERER's "ER-7MW”), the polyvinyl acetal resin. And the refractive index of the 2nd resin component was calculated
  • Example 1 the polyvinyl acetal resin and the second resin component were not compatible in the first layer.
  • Example 2 the polyvinyl acetal resin and the second resin component in the first layer form a co-continuous structure.
  • Examples 2 to 20 the polyvinyl acetal resin and the second resin component in the first layer are formed.
  • the resin component 2 formed a sea-island structure.
  • Table 1 description of blending components other than the polyvinyl acetal resin, the second resin component, and the plasticizer is omitted.

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  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Joining Of Glass To Other Materials (AREA)
  • Laminated Bodies (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

L'invention concerne un film intermédiaire pour verre feuilleté qui permet d'augmenter la rigidité et les propriétés d'isolation acoustique d'un verre feuilleté, et d'augmenter la recyclabilité du film intermédiaire. Le film intermédiaire pour verre feuilleté comprend une première couche et une seconde couche qui est stratifiée sur une première surface de la première couche. La première couche comprend une résine d'acétal de polyvinyle et un second composant de résine. La seconde couche comprend une résine d'acétal de polyvinyle. La température maximale de la tangente de l'angle de pertes du second composant de résine à l'intérieur de la première couche est de -30°C à 10°C. L'indice de réfraction du second composant de résine à l'intérieur de la première couche est compris entre 1,47 et 1,51.
PCT/JP2015/077863 2014-09-30 2015-09-30 Film intermédiaire pour verre feuilleté et verre feuilleté WO2016052671A1 (fr)

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US15/505,240 US20170266928A1 (en) 2014-09-30 2015-09-30 Intermediate film for laminated glass, and laminated glass
JP2015549878A JPWO2016052671A1 (ja) 2014-09-30 2015-09-30 合わせガラス用中間膜及び合わせガラス
KR1020167027696A KR20170063431A (ko) 2014-09-30 2015-09-30 접합 유리용 중간막 및 접합 유리
MX2017002639A MX2017002639A (es) 2014-09-30 2015-09-30 Pelicula intermedia para vidrio laminado, y vidrio laminado.
EP15845570.9A EP3202728A4 (fr) 2014-09-30 2015-09-30 Film intermédiaire pour verre feuilleté et verre feuilleté
CN201580036823.2A CN106660867A (zh) 2014-09-30 2015-09-30 夹层玻璃用中间膜及夹层玻璃
BR112017003531A BR112017003531A2 (pt) 2014-09-30 2015-09-30 película intermediária para vidro laminado, e vidro laminado

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JP2014202616 2014-09-30
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KR102223922B1 (ko) * 2019-05-31 2021-03-04 에스케이씨 주식회사 접합용 적층필름 및 이를 포함하는 광투과적층체
KR102253130B1 (ko) 2019-11-13 2021-05-14 에스케이씨 주식회사 플라스틱 중간막, 이를 포함하는 적층체 및 이를 포함하는 이동수단
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MX2017002652A (es) 2017-05-30
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WO2016052670A1 (fr) 2016-04-07
US20170266927A1 (en) 2017-09-21
US20170266928A1 (en) 2017-09-21
MX2017002639A (es) 2017-06-07
CN106660867A (zh) 2017-05-10
EP3202728A4 (fr) 2018-06-27
JPWO2016052670A1 (ja) 2017-07-13
JPWO2016052671A1 (ja) 2017-07-13
KR20170063430A (ko) 2017-06-08
EP3202736A1 (fr) 2017-08-09

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